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Chromosome 1, trisomy 1q42 qter
Known as:
Duplication 1q42 qter
, Trisomy 1q42 qter
National Institutes of Health
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Related topics
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2 relations
Broader (2)
Chromosomes, Human, Pair 1
Trisomy
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Esophageal stenosis in a child presenting a de novo 7q terminal deletion.
P. Zen
,
M. Riegel
,
+4 authors
G. Paskulin
European Journal of Medical Genetics
2010
Corpus ID: 11343714
2002
2002
Deleción terminal del 11q (síndrome de jacobsen) asociada a atresia duodenal con páncreas anular
N. González
,
S. P. Espuñes
,
+4 authors
D. B. Fernández
2002
Corpus ID: 72356635
1995
1995
Genetic linkage mapping of the dehydroepiandrosterone sulfotransferase (STD) gene on the chromosome 19q13.3 region.
F. Durocher
,
J. Morissette
,
I. Dufort
,
J. Simard
,
V. Luu‐The
Genomics
1995
Corpus ID: 40839034
In the human liver and adrenal, there is a single hydroxysteroid sulfotransferase, which catalyzes the transformation of…
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1991
1991
Fine Mapping of Probes in the Adenomatous Polyposis Coli Region of Chromosome 5 by In Situ Hybridization
Sarah V. Williams
,
T. Jones
,
+9 authors
D. Sheer
Genes, Chromosomes and Cancer
1991
Corpus ID: 45146300
The gene for adenomatous polyposis coli has been localized to 5q21–22. We have mapped six probes from this region using isotopic…
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1986
1986
Morphology alone does not make an isochromosome
S. Schmutz
,
E. Pinno
Human Genetics
1986
Corpus ID: 42159413
SummaryIsochromosomes are chromosomes with genetically identical arms. Chromosomes morphologically similar to isochromosomes can…
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